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Confidence bounds for nonlinear dose-response relationships

机译:非线性剂量反应关系的置信界

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An important aim of drug trials is to characterize the dose-response relationship of a new compound. Such a relationship can often be described by a parametric (nonlinear) function that is monotone in dose. If such a model is fitted, it is useful to know the uncertainty of the fitted curve. It is well known thatWald confidence intervals are based on linear approximations and are often unsatisfactory in nonlinear models. Apart from incorrect coverage rates, they can be unreasonable in the sense that the lower confidence limit of the difference to placebo can be negative, even when an overall test shows a significant positive effect. Bootstrap confidence intervals solve many of the problems of the Wald confidence intervals but are computationally intensive and prone to undercoverage for small sample sizes. In this work, we propose a profile likelihood approach to compute confidence intervals for the dose-response curve. These confidence bounds have better coverage than Wald intervals and are more precise and generally faster than bootstrap methods. Moreover, if monotonicity is assumed, the profile likelihood approach takes this automatically into account. The approach is illustrated using a public dataset and simulations based on the Emax and sigmoid Emax models. Copyright (C) 2015 John Wiley & Sons, Ltd.
机译:药物试验的一个重要目的是表征新化合物的剂量反应关系。这种关系通常可以用剂量单调的参数(非线性)函数来描述。如果拟合了这样的模型,了解拟合曲线的不确定性将很有用。众所周知,瓦尔德置信区间是基于线性逼近的,并且在非线性模型中通常不令人满意。除了覆盖率不正确外,就安慰剂差异的置信度下限可能为负(即使整体测试显示出明显的积极效果)而言,它们可能是不合理的。自举置信区间解决了Wald置信区间的许多问题,但计算量大,对于小样本量,容易出现覆盖不足的情况。在这项工作中,我们提出了一种轮廓似然法来计算剂量反应曲线的置信区间。这些置信范围比Wald间隔具有更好的覆盖范围,并且比自举方法更精确,通常更快。此外,如果假设为单调性,则轮廓似然法会自动考虑这一点。使用公共数据集和基于Emax和S型Emax模型的仿真说明了该方法。版权所有(C)2015 John Wiley&Sons,Ltd.

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